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Midnolin is a confirmed genetic risk factor for Parkinson’s disease
OBJECTIVE: Genetic analysis of patients with familial Parkinson’s disease (PD) identified many causative genes. However, the majority of PD cases are sporadic, and the mechanisms of onset still remain unclear. Previously, we found that Midnolin (MIDN) is associated with PD in a Yamagata (Japan) coho...
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| Publicado no: | Ann Clin Transl Neurol |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6856597/ https://ncbi.nlm.nih.gov/pubmed/31588691 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.50914 |
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